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M 944 (Divalproex Sodium Delayed-Release 250 mg)

Pill with imprint M 944 is Blue, Round and has been identified as Divalproex Sodium Delayed-Release 250 mg. It is supplied by Mylan Pharmaceuticals Inc.

Divalproex sodium is used in the treatment of bipolar disorder; mania; epilepsy; migraine prevention and belongs to the drug class fatty acid derivative anticonvulsants. When treating epilepsy and manic episodes associated with bipolar disorder: There is positive evidence of human fetal risk during pregnancy. When treating migraine: Not for use in pregnancy. Divalproex sodium 250 mg is not a controlled substance under the Controlled Substances Act (CSA).

Images for M 944

Divalproex sodium delayed-release 250 mg M 944
Divalproex sodium delayed-release 250 mg M 944
Divalproex sodium delayed-release 250 mg M 944

Divalproex Sodium Delayed-Release

Imprint
M 944
Strength
250 mg
Color
Blue
Size
11.00 mm
Shape
Round
Availability
Prescription only
Drug Class
Fatty acid derivative anticonvulsants
Pregnancy Category
D - Positive evidence of risk - When treating epilepsy and manic episodes associated with bipolar disorder, X - Not for use in pregnancy - When treating migraine
CSA Schedule
Not a controlled drug
Labeler / Supplier
Mylan Pharmaceuticals Inc.
Inactive Ingredients
ferrosoferric oxide, silicon dioxide, copovidone, croscarmellose sodium, FD&C Blue No. 2, FD&C Yellow No. 6, hypromelloses, lactose monohydrate, methacrylic acid - ethyl acrylate copolymer (1:1) type a, microcrystalline cellulose, polydextrose, polyethylene glycol, polysorbate 80, polyvinyl alcohol, propylene glycol, sodium hydroxide, magnesium silicate, titanium dioxide, triacetin, triethyl citrate

Note: Inactive ingredients may vary.

Labelers / Repackagers

NDC Code Labeler / Repackager
00378-1044 (Discontinued) Mylan Pharmaceuticals Inc.
51079-0474 (Discontinued) UDL Laboratories Inc.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.